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Integrated Medicine - Prevention Programs
Urinalysis
Urinalysis can reveal diseases that
have gone unnoticed because they do not produce striking signs or
symptoms. Examples include diabetes mellitus, various forms of glomerulonephritis, and chronic urinary tract infections.
The most cost-effective device used to
screen urine is a paper or plastic dipstick. This microchemistry system
has been available for many years and allows qualitative and
semi-quantitative analysis within one minute by simple but careful
observation. The color change occurring on each segment of the strip is
compared to a color chart to obtain results. However, a careless doctor,
nurse, or assistant is entirely capable of misreading or misinterpreting
the results. Microscopic urinalysis requires only a relatively
inexpensive light microscope.
It has
been called the golden elixir of life. It still holds much
information for those who know how to look for it. The most
cost-effective device used to screen urine is a paper or plastic
dipstick. This microchemistry system has been available for many years
and allows qualitative and semi-quantitative analysis within one minute
by simple but careful observation. The color change occurring on each
segment of the strip is compared to a color chart to obtain results.

METHODS
OF URINE COLLECTION
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Random |
Taken at any time of day with no precautions regarding
contamination. The sample may be dilute, isotonic, or hypertonic
and may contain white cells, bacteria, and squamous epithelium
as contaminants.
In females, the specimen may contain vaginal contaminants such
as trichomonads, yeast, and during menses, red cells.
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Early morning |
Early morning collection of the sample before ingestion of any
fluid. This is usually hypertonic and reflects the ability of
the kidney to concentrate urine during dehydration which occurs
overnight. If all fluid ingestion has been avoided since 6 p.m.
the previous day, the specific gravity usually exceeds 1.022 in
healthy individuals. |
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Mid stream Clean catch |
Collected after cleansing the external urethral meatus. A cotton
sponge soaked with benzalkonium hydrochloride is useful and
non-irritating for this purpose.
First half of the bladder urine is discarded and the collection
vessel is introduced into the urinary stream to catch the last
half
First half of the stream serves to flush contaminating cells and
microbes from the outer urethra prior to collection |
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Catheterization of the bladder |
Only in special circumstances, i.e., in a comatose or confused
patient
Risks introducing infection and traumatizing the urethra and
bladder, producing iatrogenic infection or hematuria. |
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Suprapubic transabdominal needle aspiration of the bladder |
Provides the purest sampling of bladder urine
Good method for infants and small children. |
MACROSCOPIC URINALYSIS
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Color |
Normal, fresh urine is pale to dark yellow or amber in color
A red or red-brown (abnormal) color could be from a food dye,
eating fresh beets, a drug, or the presence of either hemoglobin
or myoglobin. If the sample contained many red blood cells, it
would be cloudy as well as red. |
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Volume |
750 to 2000 ml/24hr |
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Clarity |
Turbidity or cloudiness may be caused by excessive cellular
material or protein in the urine or may develop from
crystallization or precipitation of salts upon standing at room
temperature or in the refrigerator. Clearing of the specimen
after addition of a small amount of acid indicates that
precipitation of salts is the probable cause of tubidity |
URINE
DIPSTICK CHEMICAL ANALYSIS
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pH |
The glomerular filtrate of blood plasma is usually acidified by
renal tubules and collecting ducts from a pH of 7.4 to about 6
in the final urine. However, depending on the acid-base status,
urinary pH may range from as low as 4.5 to as high as 8.0. The
change to the acid side of 7.4 is accomplished in the distal
convoluted tubule and the collecting duct. |
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Specific gravity |
Any specific gravity > 1.022 measured in a randomly collected
specimen denotes adequate renal concentration so long as there
are no abnormal solutes in the urine. (which is directly
proportional to urine osmolality which measures solute
concentration) measures urine density, or the ability of the
kidney to concentrate or dilute the urine over that of plasma.
Dipsticks are available that also measure specific gravity in
approximations. Most laboratories measure specific gravity with
a refractometer. Specific gravity between 1.002 and 1.035 on a
random sample should be considered normal if kidney function is
normal. Since the sp gr of the glomerular filtrate in Bowman's
space ranges from 1.007 to 1.010, any measurement below this
range indicates hydration and any measurement above it indicates
relative dehydration. If sp gr is not > 1.022 after a 12 hour
period without food or water, renal concentrating ability is
impaired and the patient either has generalized renal impairment
or nephrogenic diabetes insipidus. In end-stage renal disease,
sp gr tends to become 1.007 to 1.010.
Any urine having a specific gravity over 1.035 is either
contaminated, contains very high levels of glucose, or the
patient may have recently received high density radiopaque dyes
intravenously for radiographic studies or low molecular weight
dextran solutions. Subtract 0.004 for every 1% glucose to
determine non-glucose solute concentration.
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Protein |
Screening for protein is done on whole urine, but
semi-quantitative tests for urine protein should be performed on
the supernatant of centrifuged urine since the cells suspended
in normal urine can produce a falsely high estimation of
protein.
Normally, only small plasma proteins filtered at the glomerulus
are reabsorbed by the renal tubule. However, a small amount of
filtered plasma proteins and protein secreted by the nephron
(Tamm-Horsfall protein) can be found in normal urine. Normal
total protein excretion does not usually exceed 150 mg/24 hours
or 10 mg/100 ml in any single specimen. More than 150 mg/day is
defined as proteinuria. Proteinuria > 3.5 gm/24 hours is severe
and known as nephrotic syndrome.
Dipsticks detect protein by production of color with an
indicator dye, Bromphenol blue, which is most sensitive to
albumin but detects globulins and Bence-Jones protein poorly.
Precipitation by heat is a better semiquantitative method, but
overall, it is not a highly sensitive test.
The sulfosalicylic acid test is a more sensitive precipitation
test. It can detect albumin, globulins, and Bence-Jones protein
at low concentrations. In rough terms, trace positive results
(which represent a slightly hazy appearance in urine) are
equivalent to 10 mg/100 ml or about 150 mg/24 hours (the upper
limit of normal). 1+ corresponds to about 200-500 mg/24 hours, a
2+ to 0.5-1.5 gm/24 hours, a 3+ to 2-5 gm/24 hours, and a 4+
represents 7 gm/24 hours or greater. |
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Glucose |
Less than 0.1% of glucose normally filtered by the glomerulus
appears in urine (< 130 mg/24 hr). Glycosuria (excess sugar in
urine) generally means diabetes mellitus. Dipsticks employing
the glucose oxidase reaction for screening are specific for
glucos glucose but can miss other reducing sugars such as
galactose and fructose. For this reason, most newborn and infant
urines are routinely screened for reducing sugars by methods
other than glucose oxidase (such as the Clinitest, a modified
Benedict's copper reduction test).
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Ketones |
Ketones (acetone, aceotacetic acid, beta-hydroxybutyric acid)
resulting from either diabetic ketosis or some other form of
calorie deprivation (starvation), are easily detected using
either dipsticks or test tablets containing sodium
nitroprusside. |
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Nitrite |
A positive nitrite test indicates that bacteria may be present
in significant numbers in urine.
Gram negative rods such as E. coli are more likely to give a
positive test. |
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Leukocyte esterase |
A positive leukocyte esterase test results from the presence of
white blood cells either as whole cells or as lysed cells.
Pyuria can be detected even if the urine sample contains damaged
or lysed WBC's.
A negative leukocyte esterase test means that an infection is
unlikely and that, without additional evidence of urinary tract
infection, microscopic exam and/or urine culture need not be
done to rule out significant bacteriuria.
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MICROSCOPIC URINALYSIS
Urine
is centrifuged in a test tube forming a cohesive button at the bottom of
the tube. The sediment is resuspended in the remaining supernate and a
drop of resuspended sediment is poured onto a glass slide and
coverslipped. The sediment is first examined under the microscope at
both low and high power.
Low
power examination is used to determine the numbers of casts seen are
usually reported as number of each type found per low power field (LPF).
Example: 5-10 hyaline casts/L casts/LPF.
High
power examination is used to identify crystals, cells, and bacteria. The
various types of cells are usually described as the number of each type
found per average high power field (HPF). Example: 1-5 WBC/HPF.
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Red Blood Cells |
Hematuria is the presence of abnormal numbers of red cells in
urine due to: glomerular damage, tumors which erode the urinary
tract anywhere along its length, kidney trauma, urinary tract
stones, renal infarcts, acute tubular necrosis, upper and lower
urinary tract infections, nephrotoxins, and physical stress.
Red cells may also contaminate the urine from the vagina in
menstruating women or from trauma produced by bladder
catherization. Theoretically, no red cells should be found, but
some find their way into the urine even in very healthy
individuals. However, if one or more red cells can be found in
every high power field, and if contamination can be ruled out,
the specimen is probably abnormal.
RBC's may appear normally shaped, swollen by dilute urine (in
fact, only cell ghosts and free hemoglobin may remain), or
crenated by concentrated urine. Both swollen, partly hemolyzed
RBC's and crenated RBC's are sometimes difficult to distinguish
from WBC's in the urine. In addition, red cell ghosts may
simulate yeast. The presence of dysmorphic RBC's in urine
suggests a glomerular disease such as a glomerulonephritis.
Dysmorphic RBC's have odd shapes as a consequence of being
distorted via passage through the abnormal glomerular structure.
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White blood cells |
Pyuria refers to the presence of abnormal numbers of leukocytes
that may appear with infection in either the upper or lower
urinary tract or with acute glomerulonephritis. Usually, the
WBC's are granulocytes. White cells from the vagina, especially
in the presence of vaginal and cervical infections, or the
external urethral meatus in men and women may contaminate the
urine. If two or more leukocytes per each high power field
appear in non-contaminated urine, the specimen is probably
abnormal. |
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Epithelial cells |
Renal tubular epithelial cells, usually larger than
granulocytes, contain a large round or oval nucleus and normally
slough into the urine in small numbers.
However, with nephrotic syndrome and in conditions leading to
tubular degeneration, the number sloughed is increased. When
lipiduria occurs, these cells contain endogenous fats. When
filled with numerous fat droplets, such cells are called oval
fat bodies. Oval fat bodies exhibit a "Maltese cross"
configuration by polarized light microscopy.
Transitional epithelial cells from the renal pelvis, ureter, or
bladder have more regular cell borders, larger nuclei, and
smaller overall size than squamous epithelium.
Renal tubular epithelial cells are smaller and rounder than
transitional epithelium, and their nucleus occupies more of the
total cell volume.
Squamous epithelial cells from the skin surface or from the
outer urethra can appear in urine. Their significance is that
they represent possible contamination of the specimen with skin
flora. |
|
Casts |
Urinary casts are formed only in the distal convoluted tubule (DCT)
or the collecting duct (distal nephron). The proximal convoluted
tubule (PCT) and loop of Henle are not locations for cast
formation.
Hyaline casts are composed primarily of a mucoprotein
(Tamm-Horsfall protein) secreted by tubule cells. Even with
glomerular injury causing increased glomerular permeability to
plasma proteins with resulting proteinuria, most matrix or
"glue" that cements urinary casts together is Tamm-Horsfall
mucoprotein, although albumin and some globulins are also
incorporated.
The factors which favor protein cast formation are low flow
rate, high salt concentration, and low pH, all of which favor
protein denaturation and precipitation, particularly that of the
Tamm-Horsfall protein. Protein casts with long, thin tails
formed at the junction of Henle's loop and the distal convoluted
tubule are called cylindroids. Hyaline casts can be seen even in
healthy patients.
Red blood cells may stick together and form red blood cell
casts. Such casts are indicative of glomerulonephritis, with
leakage of RBC's from glomeruli, or severe tubular damage.
White blood cell casts are most typical for acute
pyelonephritis, but they may also be present with
glomerulonephritis. Their presence indicates inflammation of the
kidney, because such casts will not form except in the kidney.
When cellular casts remain in the nephron for some time before
they are flushed into the bladder urine, the cells may
degenerate to become a coarsely granular cast, later a finely
granular cast, and ultimately, a waxy cast. Granular and waxy
casts are be believed to derive from renal tubular cell casts.
Broad casts are believed to emanate from damaged and dilated
tubules and are therefore seen in end-stage chronic renal
disease.
The so-called telescoped urinary sediment is one in which red
cells, white cells, oval fat bodies, and all types of casts are
found in more or less equal profusion. The conditions which may
lead to a telescoped sediment are: 1) lupus nephritis 2)
malignant hypertension 3) diabetic glomerulosclerosis, and 4)
rapidly progressive glomerulonephritis. In end-stage kidney
disease of any cause, the urinary sediment often becomes very
scant because few remaining nephrons produce dilute urine.
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Bacteria |
Bacteria are common in urine specimens because of the abundant
normal microbial flora of the vagina or external urethral meatus
and because of their ability to rapidly multiply in urine
standing at room temperature. Therefore, microbial organisms
found in all but the most scrupulously collected urines should
be interpreted in view of clinical symptoms.
Diagnosis of bacteriuria in a case of suspected urinary tract
infection requires culture. A colony count may also be done to
see if significant numbers of bacteria are present. Generally,
more than 100,000/ml of one organism reflects significant bacteriuria. Multiple organisms reflect contamination. However,
the presence of any organism in catheterized or suprapubic tap
specimens should be considered significant.
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Yeast |
Yeast cells may be contaminants or represent a true yeast
infection. They are often difficult to distinguish from red
cells and amorphous crystals but are distinguished by their
tendency to bud. Most often they are Candida, which may colonize
bladder, urethra, or vagina
|
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Crystals |
Common crystals seen even in healthy patients include calcium
oxalate, triple phosphate crystals and amorphous phosphates.
Very uncommon crystals include: cystine crystals in urine of
neonates with congenital cystinuria or severe liver disease,
tyrosine crystals with congenital tyrosinosis or marked liver
impairment, or leucine crystals in patients with severe liver
disease or with maple syrup urine disease. Oxalate crystals in
urine Triple phosphate crystals in urine Cystine crystals in
urine |
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Miscellaneous |
Unidentifiable objects may find their way into a specimen,
particularly those that patients bring from home.
Spermatozoa can sometimes be seen.
Rarely, pinworm ova may contaminate the urine.
In Egypt, ova from bladder infestations with schistosomiasis may
be seen. |
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INTERFERING DISEASES OR SUBSTANCES |
CHARACTERIZATION |
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Changes occurring if there is a time delay after collection to
analysis |
Generally, urinalysis may not reflect the findings of absolutely
fresh urine if the sample is > 1 hour old
1) Decreased clarity due to crystallization of solutes
2) Rising pH
3) Loss of ketone bodies
4) Loss of bilirubin
5) Dissolution of cells and casts
6) Overgrowth of contaminating microorganisms |
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An unusual complication from a functioning indwelling urethral
catheter: case report of an abdominal mass.
Keys RH Jr, Spreen SA, Evans AT. |
J Urol 1976 Aug;116(2):257-8 Abstract quote
A heretofore unreported complication from an indwelling catheter
is presented. A catheter bulb became incarcerated in a bladder
diverticulum and was misdiagnosed subsequently as an
incarcerated umbilical hernia. The probable pathophysiological
mechanism by which this event occurred is discussed. |
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Catheter-related injuries as cause of acute surgical condition
within abdomen.
Sagalowsky A. |
Urology 1979 Mar;13(3):261-3 Abstract quote
Three cases of an acute surgical condition within the abdomen
secondary to complications of chronic urethral catheters are
reported. Common factors in the history and varying mechanisms
for the injuries are discussed. Need for including
catheter-related injuries in the differential diagnosis of an
acute surgical condition of the abdomen is emphasized. |
|
Peritonitis and abdominal free air due to intraperitoneal
bladder perforation associated with indwelling urethral catheter
drainage.
Merguerian PA, Erturk E, Hulbert WC Jr, Davis RS, May A, Cockett
AT. |
J Urol 1985 Oct;134(4):747-50 Abstract quote
Perforation of the bladder related to long-term indwelling Foley
catheter drainage is a rare and serious complication.
We report 2 cases of bladder perforation leading to generalized
peritonitis and free intraperitoneal air. These cases
re-emphasize the importance of considering bladder perforation
in the differential diagnosis of the acute abdomen and of
performing a complete abdominal exploration when the site of
perforation is not easily detectable. |
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Pressure ulcers: an unusual complication of indwelling urethral
catheter.
Sivaraman Nair KP, Taly AB, Roopa N, Murali T.
Department of Psychiatric and Neurological Rehabilitation,
National Institute of Mental Health and Neurosciences,
Bangalore, India. |
Spinal Cord 2001 Apr;39(4):234-6 Abstract quote
INTRODUCTION: Pressure ulcers are common among patients with
spinal cord disorders (SCD) and occur due to unrelieved pressure
on soft tissues.
CASE REPORTS: Two ladies with paraplegia following acute
transverse myelitis developed pressure ulcers over medial
aspects of thighs due to indwelling urethral catheter. Absence
of sensation, weakness of both legs and lack of knowledge about
catheter care contributed to ulcer formation.
CONCLUSION: Indwelling urethral catheter may unusually result in
pressure ulcers over the thighs in patients with SCD. Among
health professionals involved in the care of these subjects
awareness is essential for preventing this complication. |
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Effect of a single-use sterile catheter for each void on the
frequency of bacteriuria in children with neurogenic bladder on
intermittent catheterization for bladder emptying.
Schlager TA, Clark M, Anderson S.
Department of Pediatrics, University of Virginia Health System,
Charlottesville, Virginia. |
Pediatrics 2001 Oct;108(4):E71 Abstract quote
The frequency of bacteriuria is high in children with neurogenic
bladder on intermittent catheterization for bladder emptying. In
an effort to decrease bacteriuria, we examined whether the
method of catheter care was responsible for the high rate of
bacteriuria. For this, the frequency of bacteriuria was examined
in the same patient on single-use sterile catheters and on
reused clean catheters.
Methods. A prospective, randomized, crossover trial was
conducted with 10 patients who were randomized to 4 months of a
new, sterile catheter for intermittent catheterization and 4
months of reuse of a clean catheter for intermittent
catheterization. Each week, a urine sample was collected and
symptoms of infection and medication use were recorded. Results.
A total of 158 urine samples were collected during 164
patient-weeks on the new catheter method for each void; 115
(73%) were positive for a pathogen. Of the 161 samples collected
during 169 patient-weeks on the standard, reuse method for
voiding, 123 (76%) were positive (115 [73%] of 158 vs 123 [76%]
of 161). Escherichia coli was the most common pathogen detected
during both method periods.
Conclusion. A new, sterile catheter for each void did not
decrease the high frequency of bacteriuria in patients with
neurogenic bladder on intermittent catheterization. |
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Rapid Spot Tests for Detecting the Presence of Adulterants in
Urine Specimens Submitted for Drug Testing
Amitava Dasgupta, PhD, Amer Wahed, MD, and Alice Wells, MT(ASCP) |
Am J Clin Pathol 2002;117:325-329 Abstract quote
Several adulterants are used to mask tests for abused drugs in
urine. Adulterants such as "Klear" and "Whizzies" contain
potassium nitrite, and "Urine Luck" contains pyridinium
chlorochromate (PCC). The presence of these adulterants cannot
be detected by routine specimen integrity checks (pH, specific
gravity, and temperature).
We developed rapid spot tests for detecting these adulterants in
urine. Addition of 3% hydrogen peroxide in urine adulterated
with PCC caused rapid formation of a dark brown color. In
contrast, unadulterated urine turned colorless when hydrogen
peroxide was added. When urine contaminated with nitrite and 2
to 3 drops of 2N hydrochloric acid were added to 2% aqueous
potassium permanganate solution, the dark pink permanganate
solution turned colorless immediately with effervescence. Urine
contaminated with nitrite liberated iodine from potassium iodide
solution in the presence of 2N hydrochloric acid. Urine
adulterated with PCC also liberated iodine from potassium iodide
in acid medium but did not turn potassium permanganate solution
colorless. Urine specimens from volunteers and random urine
samples that tested negative for drugs did not cause
false-positive results.
These rapid spot tests are useful for detecting adulterated
urine to avoid false-negative drug tests. |
Henry
JB. Clinical Diagnosis and Management by Laboratory Methods. Twentieth
Edition. WB Saunders. 2001.
Rosai J. Ackerman's Surgical Pathology. Ninth Edition. Mosby 2004.
Sternberg S. Diagnostic Surgical Pathology. Fourth Edition. Lipincott
Williams and Wilkins 2004.
Robbins Pathologic Basis of Disease. Seventh Edition. WB Saunders 2005.
DeMay RM. The Art and Science of Cytopathology. Volume 1 and 2. ASCP
Press. 1996.
Weedon D. Weedon's Skin Pathology Second Edition. Churchill Livingstone.
2002
Fitzpatrick's Dermatology in General Medicine. 5th Edition. McGraw-Hill.
1999.
Weiss SW and Goldblum JR. Enzinger and Weiss's Soft Tissue Tumors.
Fourth Edition. Mosby 2001.
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